A new translocation t(9;11)(q34;p15) fuses NUP98 to a novel homeobox partner gene, PRRX2, in a therapy-related acute myeloid leukemia

This publication has 7 references indexed in Scilit:

• The Oncogene Nup98-HOXA9 Induces Gene Transcription in Myeloid Cells
  Published by Elsevier ,2004
• NUP98 gene fusions in hematologic malignancies
  Leukemia, 2001
• Human PRRX1 and PRRX2 genes: cloning, expression, genomic localization, and exclusion as disease genes for Nager syndrome
  Mammalian Genome, 2000
• The Sonic Hedgehog–Patched–Gli Pathway in Human Development and Disease
  American Journal of Human Genetics, 2000
• NUP98 Is Fused to PMX1 Homeobox Gene in Human Acute Myelogenous Leukemia With Chromosome Translocation t(1;11)(q23;p15)
  Blood, 1999
• Fusion of the nucleoporin gene NUP98 to HOXA9 by the chromosome translocation t(7;11)(p15;p15) in human myeloid leukaemia
  Nature Genetics, 1996
• The peptide repeat domain of nucleoporin Nup98 functions as a docking site in transport across the nuclear pore complex
  Cell, 1995